Ballicules › Drugs › Phendimetrazine
What it is Norepinephrine-releasing sympathomimetic and prodrug of phenmetrazine; brief adjunct for weight management.
Why this one Conversion to phenmetrazine brings substantial stimulant and abuse liability with little role beyond short-term appetite suppression.
What limits it Blood pressure and heart rate rise; avoid cardiovascular disease and MAOIs. Tolerance and dependence limit use.
FDA label
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FDA dosing Population Start Target Max
Obesity (anorectic; indication inferred from Clinical Pharmacology — Indications section not in source data) Adults 35 mg (1 tab) BID–TID, 1 h before meals; 17.5 mg (½ tab) per dose may be adequate Lowest effective dose, BID–TID 70 mg TID (2 tabs TID)
Renal Undefined
Hepatic Undefined
Instructions Take 1 hour before meals Individualize to lowest effective dosage
Contraindications Known hypersensitivity or idiosyncratic reactions to sympathomimetics Advanced arteriosclerosis, symptomatic cardiovascular disease, moderate-severe hypertension, hyperthyroidism, glaucoma Highly nervous or agitated patients History of drug abuse Concurrent other CNS stimulants, including MAOIs
Adverse reactions CV: palpitations, tachycardia, elevated BP, ischemic events; valvular heart disease reported with some anorectics (fenfluramine/dexfenfluramine, esp. in combination) — no cases reported with phendimetrazine alone CNS: overstimulation, restlessness, insomnia, agitation, flushing, tremor, sweating, dizziness, headache, psychotic state, blurred vision GI: dry mouth, nausea, diarrhea, constipation, stomach pain GU: urinary frequency, dysuria, changes in libido
Pregnancy Undefined
Lactation Undefined
Principal risk Blood pressure and heart rate rise; short-term use only
Classes and tags
Clinical profile
Direct muscarinic antagonism 0 / 4
Mechanism of action: Phendimetrazine ballicule
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